Data / Medical devices / Stimulator, Nerve, Transcutaneous, For Pain Relief / Hong Kong
FDA-registered makers of Stimulator, Nerve, Transcutaneous, For Pain Relief in Hong Kong: 6 establishments
6 establishments in Hong Kong are registered with the FDA to make Stimulator, Nerve, Transcutaneous, For Pain Relief (product code GZJ). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Stimulator, Nerve, Transcutaneous, For Pain Relief
- Product code
- GZJ
- Country
- Hong Kong
Makers of Stimulator, Nerve, Transcutaneous, For Pain Relief in Hong Kong
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Tens Plus Industrial Co. | Hong Kong, Hong Kong | Manufacturer | 4 | June 19, 2006 | 0 | 0 | 0 | api.fda.gov |
| Tyece Limited | Kowloon, Hong Kong | Specification developer | 1 | January 7, 2004 | 0 | 0 | 0 | api.fda.gov |
| Gorgeous Beauty Equipment Manufacture Limited | Hong Kong, Hong Kong | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hebei Mita Biotechnology Limited | Hong Kong, Hong Kong | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hebei Mita Technology Limited | Hong Kong, Hong Kong | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oman Medical Beauty Manufacture Limited | Hong Kong, Hong Kong | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.